rs3198697

This is a synonymous variant in the PDXDC1 gene — it does not change the protein's amino acid sequence.

GWAS Catalog Trait Associations (10)

Genome-wide significant associations (p < 5×10⁻⁸) from the NHGRI-EBI GWAS Catalog.

fatty acid amount

Allele T
OR 0.06
p 3.0e-13
N 13,814
Large GWAS
European
Allele T
OR 0.03
p 1.0e-10
N 115,006
Large GWAS
European

triglycerides in large HDL measurement

Karjalainen MK et al. Genome-wide characterization of circulating metabolic biomarkers. Nature 628(8006):130-138 (2024)
Allele T
OR 0.03
p 5.0e-10
N 136,016
Large GWAS
multi-ancestry

insomnia

Allele T
OR 0.01
p 3.0e-9
N 1,409,137
Meta-analysisLarge GWAS
European

triglyceride measurement

Hoffmann TJ et al. A large electronic-health-record-based genome-wide study of serum lipids. Nature Genetics 50(3):401-413 (2018)
Allele C
OR
β 0.028
p 8.0e-11
N 94,674
Large GWAS
multi-ancestry
Willer CJ et al. Discovery and refinement of loci associated with lipid levels. Nature Genetics 45(11):1274-1283 (2013)
Allele C
OR
β 0.020
p 2.0e-8
N 94,595
Large GWAS
European

ClinVar annotation

Benign
1 submitter

PDXDC1-related disorder

View on ClinVar →

About PDXDC1

Enables cadherin binding activity. Predicted to be involved in carboxylic acid metabolic process. Located in Golgi apparatus. [provided by Alliance of Genome Resources, Jul 2025]

View all PDXDC1 variants →

Gene information from NCBI Gene. Variant classifications from ClinVar.

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